{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-07-22",
    "results": {
      "skip": 0,
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  "results": [
    {
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      "city": "Allentown",
      "state": "PA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {
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        "route": [
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      },
      "product_type": "Drugs",
      "event_id": "97433",
      "recalling_firm": "B BRAUN MEDICAL INC",
      "address_1": "861 Marcon Blvd",
      "address_2": "N/A",
      "postal_code": "18109-9577",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.A. Nationwide",
      "recall_number": "D-0628-2025",
      "product_description": "0.9% Sodium Chloride Injection USP, 1000 mL container, Rx only, B. Braun Medical, Inc., Bethlehem, PA 18018-3524 USA, NDC 0264-7800-09",
      "product_quantity": "47,148 containers",
      "reason_for_recall": "Presence of Particulate Matter.",
      "recall_initiation_date": "20250818",
      "center_classification_date": "20250910",
      "report_date": "20250910",
      "code_info": "Lot #: V3K770, Exp 1/31/2026"
    }
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}